Effects of progesterone and interferon tau on ovine endometrial phosphate, calcium, and vitamin D signaling†

Biol Reprod. 2022 May 17;106(5):888-899. doi: 10.1093/biolre/ioac027.

Abstract

Given recent reports of expression of postnatal mineral transport regulators at the maternal-conceptus interface during the peri-implantation period, this study tested the hypothesis that progesterone (P4) and interferon tau (IFNT) regulate phosphate, calcium, and vitamin D signaling in the ovine endometrium. Mature Rambouillet ewes (n = 24) were surgically fitted with intrauterine catheters on day 7 of the estrous cycle. Ewes received daily intramuscular injections of 50 mg of P4 in corn oil vehicle and 75 mg of progesterone receptor antagonist (RU486) in corn oil from days 8 to 15, and twice-daily intrauterine injections of either control proteins (CX) or IFNT (25 μg/uterine horn/day) from days 11 to 15 resulting in four treatment groups: P4 + CX; P4 + IFNT; RU486 + P4 + CX; and RU486 + P4 + IFNT. On day 16, ewes were hysterectomized. RU486 + P4 + CX treated ewes had lower concentrations of 25 (OH) D in plasma than P4 + CX treated ewes (P < 0.05). Endometria from ewes treated with IFNT had greater expression of FGF23 (P < 0.01), S100A9 (P < 0.05), and S100A12 (P = 0.05) mRNAs and lower expression of ADAM10 mRNA (P < 0.01) than of ewes treated with CX proteins. Expression of FGF23 mRNA was greater in endometria of ewes that received RU486 + P4 + IFNT than in ewes that received RU486 + P4 + CX (hormone × protein interaction, P < 0.05). The expression of S100G mRNA was greater in endometria of ewes that received P4 + IFNT compared to ewes that received RU486 + P4 + IFNT (P < 0.05; hormone × protein interaction, P < 0.01). These data implicate P4 and IFNT in the regulation of phosphate, calcium, and vitamin D signaling during the peri-implantation period of pregnancy and provide a platform for continued mechanistic investigations.

Keywords: calcium; endometrium; interferon tau; ovine; phosphate; placenta; progesterone; vitamin D.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcium / metabolism
  • Corn Oil / metabolism
  • Corn Oil / pharmacology
  • Endometrium / metabolism
  • Female
  • Interferon Type I* / metabolism
  • Mifepristone / pharmacology
  • Phosphates / metabolism
  • Phosphates / pharmacology
  • Pregnancy
  • Pregnancy Proteins
  • Progesterone* / metabolism
  • Progesterone* / pharmacology
  • Proteins / metabolism
  • RNA, Messenger / metabolism
  • Sheep
  • Sheep, Domestic
  • Vitamin D / pharmacology

Substances

  • Interferon Type I
  • Phosphates
  • Pregnancy Proteins
  • Proteins
  • RNA, Messenger
  • interferon tau
  • Vitamin D
  • Mifepristone
  • Progesterone
  • Corn Oil
  • Calcium